System and method for real time monitoring of a chemical sample

ABSTRACT

The disclosed system and method improve measurement of trace volatile chemicals, such as by Gas Chromatography (GC) and Gas Chromatography/Mass Spectrometry (GCMS). A first trapping system can include a plurality of capillary columns in series and a focusing column fluidly coupled to a first detector. The first trapping system can retain and separate compounds in a sample, including C3 hydrocarbons and compounds heavier than C3 hydrocarbons (e.g., up to C12 hydrocarbons, or compounds having a boiling point around 250° C.), and can transfer the compounds from the focusing column to the first detector. A second trapping system can receive compounds that the first trapping system does not retain, and can include a packed trap and two columns. The second trapping system can remove water from the sample and can separate and detect compounds including C2 hydrocarbons and Formaldehyde.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. patent applicationSer. No. 16/197,791, filed Nov. 21, 2018, the entire disclosure of whichis incorporated herein by reference in its entirety for all purposes,which claims the benefit of U.S. Provisional Patent Application No.62/589,798, filed on Nov. 22, 2017, the entire disclosure of which isincorporated herein by reference in its entirety for all purposes and ofU.S. Provisional Patent Application No. 62/727,200, filed on Sep. 5,2018, the entire disclosure of which is incorporated herein by referencein its entirety for all purposes.

FIELD OF THE DISCLOSURE

This relates to systems and methods of preconcentrating a chemicalsample and, more particularly, to a system with multiple traps ofdifferent kinds for preconcentrating and separating various compounds ofa chemical sample into separate sample streams for analysis by gaschromatography.

BACKGROUND OF THE DISCLOSURE

The analysis of volatile chemicals in air or other matrices at low tosub-PPB levels can require the preconcentration of the sample prior toinjection into a Gas Chromatograph (GC), because most detectors are notsensitive enough to analyze chemicals at the sub-PPB level. Volatilechemicals can be measured in outdoor and indoor air to determine therisk they impose on the human population living in those areas. Inaddition, many of these compounds may react with oxides of Nitrogen(NOx) in the presence of sunlight to create photochemical smog such asOzone. Comprehensive monitoring of VOCs is becoming more commonworld-wide for both of these reasons. The typical range of concernstarts as low as 0.001 PPBv for some compounds depending on theirtoxicity, carcinogenic properties, or their influence on Ozone creationrates. In order to detect compounds at these concentrations, a samplehaving a volume in the range of 0.2-1 liters may be preconcentratedresulting in a final volume in the range of 2-100 microliters prior tointroduction into a GC capillary column. This preconcentration can allowthe sample to be injected at a rate that is fast enough to achieve highchromatographic resolution using low flow capillary GC systems.

The challenge in the past has been to develop preconcentration systemsand analyzers that are able to recover compounds as light as Ethane,Ethylene and Acetylene (C2 hydrocarbons) while being able to alsorecover heavier compounds such as C12 hydrocarbons (n-Dodecane andothers) with good precision, without using cryogenic or electroniccooling. In other words, it is required in many situations topreconcentrate and analyze samples including compounds that have aboiling point range of −90° C. to 230° C. Many approaches to trappingthis range of compounds involve cooling the traps below sub-ambienttemperatures in order to increase the adsorptive strength of each trap.In general, adsorbents become roughly ten times stronger for every 35°C. they are cooled down, so cooling an already strong trap tosub-ambient temperatures makes them even stronger. Unfortunately, insome situations, cooling the traps in this way may not allow water vaporto pass through these traps. In most cases, most of the water must beeliminated prior to injection into a capillary GC because normal waterconcentrations of 0.5-3% in air (5-30 million PPB) can be too high to behandled by GCMS systems, as the performance of both the capillary columnand the mass spectrometer detector can be negatively affected. That is,the concentration of water vapor in air can overload the GC column andcan create signal suppression in the mass spectrometer. Additionally,the water must be removed without loss of polar or non-polar VOCs ofinterest in most situations.

Some approaches for measuring C2-C12 Hydrocarbons during real timeanalysis in the field can use complicated electronic cooling which maynot permit the elimination of water vapor. To remove excess water vapor,some systems can pass the initial air sample through a membrane that canabsorb and eliminate most of the water. Unfortunately, this approach mayalso eliminate polar VOCs, such as those containing oxygen (Alcohols,Ketones, Aldehydes, Esters, etc.), so these analyzers may be unable tomeasure some of the toxic chemicals found in air, and they may notrecover all compounds that have an influence on Ozone formation rates inurban air. This can prevent these polar VOCs (PVOCs) from being measuredaccurately during real time monitoring, which is problematic as PVOCscan account for up to half of the total VOC inventory in some locations.

Some water removal systems use electronic cooling to selectively freezeout the water by cooling a first trap to about −30° C. which removesmost of the water by reducing the sample stream to a dew point of −30°C. Trapping of the VOCs then occurs on a second stage trap containingmultiple adsorbents also at −20 to −30° C. Unfortunately, these systemscan take too long to cool back down after sample injection and bakeoutto perform real-time analysis with a single preconcentration system, sothese systems must use two separate systems where one is injecting,baking, and cooling while the other system is trapping the sample.Unfortunately, this adds significantly to the cost, and makes it harderto obtain good system precision as two separate systems are alternatelygenerating the data, potentially requiring separate calibrations to beperformed for both systems.

Many real-time analyzers-use two Flame Ionization Detectors (FIDs) andtwo separate columns in the GC to measure the C2-C12 Hydrocarbons,without the use of a mass spectrometer to confirm compound identities.The identification of each compound relies on maintaining a consistenttime of elution (Retention Time—RT) for each compound. Unfortunately,many air samples can include thousands of VOCs whose concentrations canvary widely based on the proximity of chemical refineries that producelighter boiling precursors for today's plastics and synthetics. Withoutthe use of mass spectrometry to identify and isolate the target VOCsfrom other interfering compounds, systems that rely on dual FIDanalyzers can suffer from positive bias as compounds are misidentified.

SUMMARY OF THE DISCLOSURE

Some embodiments of the disclosure are directed to systems and methodsincluding gas chromatography for the analysis of chemical samples, suchas chemical samples including volatile organic compounds (e.g.,compounds with boiling points between −100° C. to 250° C.).Additionally, some embodiments of the disclosure may analyze a range ofcompounds without cryogenic or electronic cooling of the component partsof those embodiments. Some embodiments of the disclosure include aMulti-Capillary Column Trapping System (MCCTS) that can include multiplecapillary columns arranged in increasing strength (i.e., chemicalaffinity for particular compounds of interest). In some embodiments,however, MCCTS may not adequately trap the lightest compounds ofinterest in air, such as C2 Hydrocarbons boiling at about −90° C., andFormaldehyde when sampling large volumes needed for reaching detectionlimits (typically 200-400 cc). Thus, some embodiments of the disclosurealso include one or more packed traps and/or capillary columns inaddition to one or more MCCTS. The packed and capillary columns of theseembodiments can fluidly couple to the MCCTS and can capture (or trap)the compounds that the MCCTS may not adequately retain (e.g., C2Hydrocarbons and Formaldehyde). These systems may include additionalcolumns to facilitate the removal of water vapor from the organiccompounds of interest (e.g., C2 Hydrocarbons and Formaldehyde).Moreover, these systems can include two or more different detectors todetect different categories of compounds. For example, the system caninclude a flame ionization detector and/or photoionization detector todetect compounds such as C2 Hydrocarbons and Formaldehyde and a massspectrometry detector to detect C3-C12 Hydrocarbons. Other detectortypes, are possible, including Pulsed Discharge Detectors (PDDs),Acoustic Detectors, and Methanizers that first convert eluting compoundsto CO2, then to Methane for more accurate quantitation by FFID.

The embodiments described in this application include numerousadvantages over other systems and techniques of conducting chemicalanalysis by gas chromatography. For example, all traps and oventemperatures can be operated at 35° C. or higher, eliminating the needfor cryogenic or electronics cooling. The use of MCCTS can eliminatemany of the deficiencies in prior art systems using packed traps forconcentrating C2-C12 compounds. For example, MCCTS can eliminatechanneling that occurs due to expansion and contraction of sorbent inpacked traps. Using much smaller adsorbent particles in the capillarytraps of MCCTS can cause MCCTS to release chemicals faster as well asclean up faster after each analysis. This can be particularly importantfor the rapid injection and cleanup of the heavier VOCs in the mixture.Thus, the MCCTS can facilitate rapid system cleanup (i.e., reset), withfar less carryover than that of systems using packed traps. Finally,dual passivated stainless steel vacuum canisters can be used to collectreal time air samples at a substantially constant rate, alternating witheach vacuum canister collecting one hour samples. Substantially constantsampling may lead to more accurate results despite any time spent bakingand cooling down traps between analyses. Each canister can collectsample for an hour when doing hourly analysis, which is an advantagerelative to systems that trap the sample directly and do not initiallycollect the sample in a canister as these systems can only sample for15-30 minutes each hour due to the requirement to desorb, bake out andcool the traps back down prior to the next sample preconcentration. Inthe system described here, one canister can be sampling for an hourwhile the other canister can be analyzed and re-evacuated in preparationfor the next one hour sampling event. Moreover, the system can be usedin a stationary laboratory where whole air samples are collected anddelivered to the lab using inert vacuum sampling containers. And someembodiments can operate in a mobile lab that can be driven to thelocation where air analysis will be performed. Finally, the system canbe used for continuous monitoring of air at permanent or semi-permanentmonitoring stations, testing for hundreds of compounds at 0.001 PPB toPPM levels, including some compounds designated in the US 1990 Clean AirAct Amendment.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates an exemplary block diagram of a system forpreconcentrating and analyzing various compounds in a chemical sample bygas chromatography according to one example of the disclosure.

FIG. 2A illustrates one example of a first trapping system according tothe disclosure.

FIG. 2B illustrates an exemplary second trapping system according to thedisclosure.

FIG. 2C illustrates an exemplary system for preconcentrating andanalyzing one or more groups of compounds within a chemical sampleaccording to the disclosure.

FIG. 3 illustrates an exemplary process for analyzing a chemical sampleaccording to the disclosure.

FIG. 4 illustrates an exemplary system for preconcentrating andanalyzing one or more groups of compounds within a chemical sampleaccording to the disclosure.

FIG. 5 illustrates an exemplary process for analyzing a chemical sampleaccording to the disclosure.

DETAILED DESCRIPTION

In the following description, reference is made to the accompanyingdrawings which form a part hereof, and in which it is shown by way ofillustration specific examples that can be practiced. It is to beunderstood that other examples can be used and structural changes can bemade without departing from the scope of the examples of the disclosure.

FIG. 1 illustrates an exemplary block diagram of a system 100 forpreconcentrating and analyzing various compounds in a chemical sample bygas chromatography according to one example of the disclosure. Thesystem 100 of FIG. 1 includes a sample 102, a first trapping system 104,a first detector 110, a second trapping system 124, and one or moresecond detector(s) 120. In some embodiments, additional or alternativecomponents are possible. Further, system 100 can be modified to includeone or more of the components described below with reference to FIGS.2A-C.

In the system 100 illustrated in FIG. 1 , sample 102 comprises a gasinput (passed into) the system 100. For example, as described in greaterdetail with reference to FIG. 2A below, the system 100 can select aninput from a variety of different gas inputs, and the sample 102 canrefer to a single selected gas input to system 100. More specifically,the system 100 can select a gas sample 102 held (i.e., collected) in avacuum canister. As also described in greater detail below, the system100 can be designed to select from at least two such samples (e.g., toenable real-time or continuous sampling). As can be appreciated by oneof skill in the art, existing vacuum systems can collect samples ofambient air (i.e., gas samples) into more than one inert vacuum canisterat a constant flow rate to facilitate continuous (or approximatelycontinuous) sampling. For example, the system 100 is capable ofoperating in conjunction with two vacuum canisters (or vacuum systems),not shown in FIG. 1 , to collect sample 102 as an average collected intothe canisters over a predefined period of time (e.g., one hour).Further, the system 100 can conduct an analysis according to a userdefined schedule (e.g., hourly) by collecting a first real time sampleduring a first time period (e.g., a first hour) at a constant flow rate.Then, during the following (second) time period (e.g., a second hour),the system 100 can collect a second real time sample, also at a constantflow rate, while the system 100 analyzes the first real time sample thatit collected during the first time period. After the system 100 analyzesthe first real time sample, it can evacuate the first vacuum canisterand it can, based on user instructions, begin to collect a third realtime sample over a third time period (e.g., a third hour), possiblywhile the system analyzes the second real time sample that is collectedduring the second time period (or second hour). And as one skilled inthe art can appreciate, the system 100 could be programmed to collectand analyze samples (i.e., by gas chromatography) with a delay betweensubsequent analyses or with time periods that are greater than one hour(e.g., 2, 3, 4, 6, or 8 hours, and the like).

Thus, the system 100 can collect a sample 102 that accounts for (e.g.,is an average that includes) even short-term fluctuations in theconcentrations of volatile organic compounds in the sampled air masswhile the system 100 collects sample 102 during the user-defined timerperiod (e.g., an hourly average). In other words, a user may program thesystem 100 with an analysis frequency (i.e., a time period forcollecting samples) greater than, or less than, one hour. For example,instead of sampling an average concentration every hour, the system 100is also able to analyze the sample 102 once every 2, 3, 4, 6, 8, or 12hours or longer. And because the real time samplers are still collectingfor the entire integration period (e.g., over six consecutive hours) atrue average of the concentration of chemicals in the air over anysuitable integration period can be obtained. And, as can be appreciated,an increase in the duration of the integration period can correspond toa decrease in the total amount of GC analysis required (i.e., theanalysis occurring at the end of each integration period). Asappreciated in the art, components for gas chromatography may work for alimited amount of time before those components require maintenance(i.e., down-time). Therefore, collecting sample 102 in collectiondevices (e.g., vacuum canisters) to allow the system 100 to operate withfewer total gas chromatography analyses over a specified period of timeextends the time that the system 100 can operate before it requiresroutine maintenance (i.e., down-time).

As illustrated in FIG. 1 , system 100 can further include a firsttrapping system 104. As described in more detail below with reference toFIGS. 2-3 , the system 100 includes first trapping system 104 to retain(capture) a specific group of compounds (e.g., C3-C12 hydrocarbons) inthe sample 102 and to analyze those compounds it retains by gaschromatography. As is also described in greater detail below withreference to FIG. 2A, embodiments of the first trapping system 104include two or more multi-capillary column traps to retain a subset ofthe compounds that may be present in the sample 102. For example, basedon the composition of the air (or other gas) sampled by the system 100,the sample 102 can include C3 hydrocarbons and heavier compounds (e.g.,C3-C12 hydrocarbons) that the first trapping system 104 retains. And thesample 102 can further include lighter compounds (e.g., C2 hydrocarbons,Formaldehyde or water vapor) that pass through the first trapping system104. Thus, if the sample 102 includes C3-C12 hydrocarbons, the firsttrapping system 104 can separate the sample 102 (i.e., separates thecompounds of interest within the sample 102) into two groups; andretains a group of compounds in the sample 102 (e.g., C3-C12hydrocarbons) and communicates the rest of the sample 102 (e.g., watervapor, C2 hydrocarbons, and Formaldehyde) downstream for gaschromatography analysis in the second trapping system 124.

As shown in FIG. 1 , the first trapping system 104 is fluidly coupled toa first detector 110. As described in greater detail with reference toFIG. 2A below, the first trapping system 104 preconcentrates thecompounds it retains from the sample 102 to facilitate the analysis ofthe distribution of those retained compounds by gas chromatography. Sothe system 100 shown in FIG. 1 can include a gas chromatography focusingcolumn (not shown), either as part of the first trapping system 104, orbetween the first trapping system 104 and the first detector 110. Thefirst detector 110 can receive the compounds retained by the firsttrapping system (e.g., C3-C12 hydrocarbons) as part of a gaschromatography analysis of those compounds. And as can be appreciated byone of skill in the art, gas chromatography analysis of the compoundsretained by the first trapping system 104 can include a preconcentrationphase to facilitate optimal (rapid) transfer of the compounds to thefirst detector 110. That is, the first trapping system 104 can pass thecompounds it retained from the sample 102 through a focusing trap beforethey are transferred to the first detector 110 for chemical analysis bygas chromatography. Examples of the first detector 110 of the system 100include a Mass Spectrometry detector. The system 100 can further includea chemical separation column, such as a GC column in the flow pathbetween the first trapping system 104 and the first detector 110.Because the water vapor and bulk gases may not be retained by the firsttrapping system 104, these compounds do not enter the first detector 110during gas chromatography analysis of the compounds that the firsttrapping system 104 retained from the sample 102 (e.g., the C3-C12hydrocarbons).

The exemplary system 100 further includes a second trapping system 124,as will be described in more detail below with reference to FIGS. 2-3 .In many embodiments, the second trapping system 124 traps (retains) andpreconcentrates the lighter compounds of the chemical sample for gaschromatography analysis, such as C2 hydrocarbons and Formaldehyde.Additionally, one or more other compounds such as water and bulk gas canpass through part of the first trapping system 104 to enter the secondtrapping system 124. The second trapping system 124 separates thenon-polar sample compounds, such as the C2 hydrocarbons, from the polarcompounds, such as Formaldehyde and water vapor, and can transfer the C2hydrocarbons to a second column (e.g., the PLOT column 222B described indetail below with reference to FIG. 2B) without also transferring asubstantial portion of the water vapor. During the transfer of the C2hydrocarbons to the second column (e.g., PLOT column 222B of FIG. 2Bbelow) the C2 hydrocarbons (e.g., Ethylene, Acetylene, and Ethane) canseparate from one another (i.e., resolve into separate chromatographypeaks) so that when they ultimately elute from the second column (e.g.,PLOT column 222B of FIG. 2B), they can be measured separately from oneanother. The transfer of C2 hydrocarbons through the polar column to thesecond column can stop before elution of the C2 hydrocarbons. Then thesecond trapping system 124 separates the water vapor (or most the watervapor) from the other polar compounds (e.g., Formaldehyde), so the watervapor can be expelled from the system 100. The second trapping system124 can then transfer the remaining polar compounds (e.g., Formaldehyde)to the second column (i.e., PLOT column 222B of FIG. 2B). The system100, or the second trapping system 124, can preheat the second (strong)column (not shown in FIG. 1 ) and after a desorption temperature isattained, transfer the compounds of interest (e.g., C2 hydrocarbons andFormaldehyde) from the second column to the second detector 120, withthe three C2 hydrocarbons and Formaldehyde being separated (resolved)from one another so they can be measured accurately. As can beappreciated by one skilled in the art, the second detector can be anyappropriate detector for performing gas chromatography such as a flameionization detector. In one example, however, the second detector 120includes a photoionization detector (PID) in series with a flameionization detector such that the compounds transferred to the seconddetector 120 first enter the PID and then the FID (according to theseries configuration of the two detectors). In some examples, PulsedDischarge Detectors (PDD), Acoustic Detectors, or other detectors mayalso be used to optimize sensitivity and quantitation. Moreover, in someembodiments the second detector 120 may include a focusing column beforeone or more detectors.

Thus, the second trapping system 124 can transfer the C2 hydrocarbons tothe second detector 120 to perform chemical analysis of those compoundswithout allowing the water vapor to enter the second detector 120.

Thus, system 100 can be used to perform separate chemical gaschromatography analyses of a sample separated into different streams,such as C3 hydrocarbons and heavier compounds, C2 hydrocarbons (e.g.,Ethane, Ethylene, and Acetylene), and Formaldehyde while alsopreconcentrating these sample streams and removing bulk gases and watervapor from the sample. Another example of the disclosure (or thedisclosure according to another embodiment) including a gaschromatography system 200, a first trapping system 204, a secondtrapping system 224, and a system 200 including the first trappingsystem 204 and the second trapping system 224 and operation of thesesystems are described in more detail below with respect to FIGS. 2-3 .

FIG. 2A illustrates one example of a first trapping system 204 accordingto the disclosure. The first trapping system 204 shown in FIG. 2Aincludes a first multi-capillary column trap 212 and a secondmulti-capillary column trap 232. The exemplary first trapping system 204shown in FIG. 2A further includes a chemical separation column 236 and afirst detector 210. The first trapping system 204 illustrated in FIG.2A, and other embodiments of a first trapping system that may differsomewhat from the example shown in FIG. 2A without departing from thescope of the disclosure, can be similar to first trapping system 104described above with reference to FIG. 1 .

As shown in FIG. 2A, the exemplary first trapping system 204 includes amulti-way stream select valve as its sample source 202. The samplesource 202 is switchably couplable to multiple sample streams, such asinternal standard 202A, a first calibration standard 202B, a secondcalibration standard 202C, a blank gas 202D, a first real-time sample202E, and a second real-time sample 202F. Additional or alternatestreams are possible. As a specific example, the first real-time sample202E can be stored in a cylinder or vacuum canister, and the otherstreams coupled to select valve 202 could likewise be stored samples orstandards or input from some other means.

The first trap 212 and the second trap 232 can each include a pluralityof capillary columns 208A-C and 238A-C that can be configured to trap asubset of chemical compounds within a sample. For example, each of thecapillary columns 208A-C and 238A-C of the first and secondmulti-capillary column traps 212 and 232 can be internally coated by asorbent that retains one or more compounds of a chemical sample.

A capillary column can be an “open tubular” structure (e.g., a tube) foruse in GC and/or GCMS that has adsorbent (e.g., small adsorbentparticles or a thin film polymer) coating its internal walls. Thestrength of a capillary column corresponds to its affinity (or tendency)to adsorb one or more compounds within a sample allowed to flow throughthe column. For example, a low strength capillary column has arelatively low affinity to adsorb or absorb one or more compounds withinsample. And contrastingly, a high strength capillary column can haverelatively high affinity to adsorb or absorb one or more compoundswithin the same (or substantially similar) sample. The strength of acapillary column can be a function of one or more of its physicalcharacteristics (e.g., its length, its inner diameter, the adsorbentcoated on its inner walls, etc.).

As shown in FIG. 2A, the first trap 212 can include a weak column 208A,a moderate column 208B, and a strong column 208C coupled to one anotherin series. Other numbers of capillary columns are possible. The columns208A-C are fluidly coupled in order of increasing chemical affinity toone or more compounds of a chemical sample, though it is understood thatfewer or more columns of sequentially increasing chemical affinity(i.e., strength) can be used in other examples of the disclosure. Thesystem 200 can include stronger columns (e.g., 208C and 238C) to retainthe lighter compounds of a sample; the strong columns, however, may notreadily (or completely) release the heavier compounds in a sample. So,the system 200 can include one or more columns that are weaker relativeto the stronger columns that can be used in front of the strongercolumns (i.e., relative to the direction in which a sample flows whenfirst input to system 200) to trap heavier compounds in the weakercolumns and prevent (or reduce) the heavier compounds that may beotherwise trapped by the stronger columns. This arrangement in system200, of weak columns filtering heavier compounds from inputs to strongercolumns, can facilitate recovery of heavier compounds during desorption(e.g., when desorption gas flows in the direction opposite to thedirection the sample travelled during trapping).

Similarly, the second trap 232 includes a weak column 238A, a moderatecolumn 238 b, and a strong column 238C arranged in a manner similar tothe columns 208A-C of the first trap 212. Each of the columns 208A-B and238A-C of the first and second traps 212 and 232 can vary from 0.1meters in length to several (e.g., two, three or five) meters in length.Weak column 208A can be a 0.53 mm ID 100% polydimethylsiloxane column,moderate column 208B can be a 0.53 mm ID Porous Layer Open Tubular(PLOT) Q column (e.g., 0.5 to 2 meters in length), and strong column208C can be a 0.53 mm ID carbon molecular sieve PLOT column (e.g., 0.1to 4 meters in length). The first and second traps 212 and 232 caninclude capillary columns 208A-C and 238A-C that have relatively smallinner diameters (e.g., 0.021″ or less).

These column details are provided by way of example only, and it isunderstood that additional or alternative columns can be used inaccordance with the examples of the disclosure. For example, column 208C(e.g., the strongest column in trap 204) can be a very strong PLOTcolumn such as a carbon molecular sieve. In general, one or more ofcolumns 208 can be Polymer based Wall Coated Open Tubular (WCOT) columnsor Porous Layer Open Tubular (PLOT) columns. In some embodiments, thecolumns within trap 204 and trap 232 can be fluidly coupled togetherusing GC column unions, such as glass press fit unions or any low volumeconnection.

The first trap 212 further includes heater 216A, which can be anysuitable device for heating (or otherwise controlling the temperatureof) the capillary columns 208A-C within the first trap 212. For example,capillary columns 208 can be contained within an oven or a mandrel(e.g., aluminum or copper) to allow for consistent temperatures of thecolumns 208A-C whether trapping compounds (e.g., at a cool temperature,such as 20-50° C.) or back desorbing compounds (e.g., at a hottemperature, such as 100-300° C.) during cleaning or for sampleanalysis. Heating may be performed by passing an electrical currentthrough a resistive coating or sleeve on the columns or by wrappingheating wire around the columns. Alternatively, the columns 208A-C canbe heated by configuring the mandrels of columns 208A-C in physicalcontact (i.e., thermally coupling them) with a heating plate. In someexamples, heater 216 can include an external fan or blower 216B than canreduce the temperature of the oven (and thus trap 204 and/or columns208A-C) to ambient temperatures (e.g., 25° C. or 35° C.) or lower.

As illustrated in FIG. 2A, the first trapping system 204 can be fluidlycoupled to a chemical separation column 236, such as a GC column, and afirst detector 210, such as an MS detector. The chemical separationcolumn 236 and first detector 210 can receive the sample concentrated bythe first trapping system 2A.

As shown in FIG. 2A, the first trap 212 fluidly couples to the samplesource 202 and to the second trap 232 at a first end that is proximateto the weak column 208 a of the first trap 212. Thus, during a firsttrapping stage, the sample flows in a first direction from the weakcolumn 208 a towards the strong column 208C (e.g., through the firsttrap 212 from left to right as illustrated in FIG. 2A). During thisfirst trapping stage, some of the compounds of the sample (e.g., C2hydrocarbons, Formaldehyde, bulk gases, and water) are not retained bythe first trap 212. The compounds not retained by the first trap 212 areable to exit the first trap 212 for further analysis and for removal ofbulk gases and water vapor using a different trapping system, such assecond trapping system 124 or 224 described with reference to FIGS. 1and 2B-2C. The compounds that the first trap 212 does retain, however,(e.g., C3-C12 hydrocarbons) can be focused by the first trapping system204 and analyzed by the first detector 210 as will now be described.

During a desorption process, the compounds that were retained by thefirst trap 212 are able to flow in the reverse direction from the strongcolumn 208 c towards the weak column 208 a and into the second trap 232.Similarly, the compounds are able to flow in a direction from the weakcolumn 238 a of the second trap towards the strong column 238 c of thesecond trap 232 during trapping and are able to flow in the oppositedirection during desorption. This process reduces the bandwidth of thesample compounds to improve the sensitivity of the chemical analysisresults.

After desorbing the compounds from the second trap 232, the compoundscan be rapidly injected into the chemical separation column 236 and theninto the first detector 210 for chemical analysis. The first trappingsystem 204 and the second trapping system 224, described below withreference to FIGS. 2B-C, can process different sets of compounds in asubstantially simultaneous fashion. For example, while the firsttrapping system 204 and the first detector 210 process (e.g., trap,detect, and analyze) one set of compounds, the second trapping system224 and the second detector(s) 220 can process (e.g., trap, separate,concentrate, or analyze) the other compounds of the sample that were notretained by the first trapping system 204 as described below withreference to FIGS. 2B-2C.

FIG. 2B illustrates an exemplary second trapping system 224 according tothe disclosure. The second trapping system 224 includes a valve system240, pressure/flow controllers 242 and 244, a packed trap 222A, a polarcolumn 228, an input port A (coupled to an output of the first trappingsystem 104 or 204 described in greater detail with reference to FIGS.1-2A), a split port (or split vent) 226A, a PLOT column 222B, adesorption gas valve 226B, a 3-way valve 226C coupled to the polarcolumn 228, the split port 226A, and the PLOT column 222B, and one ormore second detectors 220. Additional or alternative components arepossible.

The exemplary second trapping system 224 illustrated in FIG. 2B isconfigured to trap, preconcentrate and analyze light compounds (e.g., C2hydrocarbons and Formaldehyde) that may include greenhouse gases (e.g.,Fluorocarbons and Chlorofluorocarbons) with a low boiling point (e.g.,−50° C. to −100° C.). Thus, the gas that enters inlet port A should befiltered (e.g., using first trapping system 104 or 204 or anothersuitable filter) before being allowed to enter the second trappingsystem 224.

As illustrated in FIG. 2B, the valve system 240 can include a valvecapable of controlling the fluid coupling, and fluid flow between thefirst trap 212 of the first trapping system 204, the packed trap 222A,the polar column 228, and the volume/flow controllers 242 and 244,thereby controlling the flow of the sample (or part of the sample) intoand out of various stages of system 200. For example, the valve system240 includes or is a rotary valve having a LOAD position in whichpositions 1 and 2 are connected and an INJECT position in whichpositions 2 and 3 are connected. While the valve system 240 is in theLOAD position, sample (e.g., the light compounds of a sample such as C2hydrocarbons and Formaldehyde) can be transferred from the first trap212 of the first trapping system 204 to the packed trap 222A and whilethe valve system 240 is in the INJECT position, sample can betransferred out of the packed trap 222A towards the polar column 228 andthe PLOT column 222B. Moreover, the valve system 240 can be a rotaryvalve configured to facilitate the flow of fluid through the secondtrapping system 224 (e.g., to perform a trapping process at the packedtrap 222A with valve system 240 in a LOAD position, and to perform adesorption process from packed trap 222A with the valve system 240 in anINJECT position), as described in greater detail below with reference toFIG. 2C.

As described above, the second trapping system 224 can include a packedtrap 222A. In some embodiments of the disclosure, the packed trap 222Acan be a high capacity C2/CH2O trap. That is, the packed trap 222A cancontain a strong adsorbent that can retain those chemical compounds(e.g., C2 hydrocarbons and Formaldehyde) not retained by the firsttrapping system 204 described with reference to FIG. 2A above. So,packed trap 222A may be able to trap 200-500 cc of sample or standardgas without loss of the C2 hydrocarbons or Formaldehyde that the samplemay contain and allowing enough volume of the sample to reach requireddetection limits for these compounds.

Further, the exemplary second trapping system 224 illustrated in FIG. 2Bincludes a polar column 228, such as an ionic liquid column or other gaschromatography column with suitable retention characteristics for polarcompounds. The polar column 228 is able to substantially retain polarcompounds present in a sample (e.g., Formaldehyde and water vapor) and,at substantially equal operating temperature, substantially pass (i.e.,not retain) non-polar compounds (e.g., C2 hydrocarbons). The polarcolumn 228 can be between approximately 5-30 meters in length, with aninternal diameter of approximately 0.25 to 0.53 millimeters (e.g.,approximately 0.32 millimeters).

As also mentioned above, the second trapping system 224 can include aPLOT column 222B with a relatively strong (e.g., high chemical affinity)sorbent to retain compounds of interest and focus the compounds prior todetection via a second detector 220 (e.g., flame ionization detectorand/or a photoionization detector). In some embodiments, the PLOT column222B is a strong carbon molecular sieve or Carboxen PLOT column. ThePLOT column 222B can be approximately 10 meters in length and can havean internal diameter of approximately 0.53 millimeters. One end of thePLOT column 222B can be fluidly coupled with the second detector(s) 220.

The second trapping system 224 can also include a 3-way valve 226C asshown in FIG. 2B. The 3-way valve 226C can be a 3-way solenoid valvethat can operate to selectively connect the polar column 228 with thePLOT column 222B or to connect the polar column 228 with the split port226A.

Additionally, the system can include a flame ionization detector and/ora photoionization detector as the second detector(s) 220 and it canreceive (and measure) the compounds from the PLOT column 222B during adesorption process. The one or more second detector(s) 220 can be aphotoionization detector in series with a flame ionization detector. Inmany situations, the flame ionization detector can detect C2hydrocarbons with high reliability and the photoionization detector candetect Formaldehyde with high reliability. Thus, it should beappreciated that “the second detector(s) 220” refers to one of thesedetectors, the two of these detectors arranged in series, or some otherdetector suitable to detect the compounds of interest in a particularsample.

The packed trap 222A can be fluidly coupled to the polar column 228through valve system 240 or a switching valve, using Dean Switching oraccording to other valve switching techniques and configurations. Forexample, during desorption, a six-port two-position switching valve canoperate to place one end of the packed trap 222A in fluid communicationwith a one end of the polar column 228. Thus, during a desorptionprocess of the second trapping system 224; one or more compounds can betransferred from the packed trap 222A to the polar column 228 and thePLOT column 222B. During this time, the 3-way valve 226C can open theflow path between the polar column 228 and the PLOT column 222B whileclosing the path between the polar column 228 and the split port 226A.

With the valve system 240 and the 3-way valve 226C configured asdescribed above and after preheating the packed trap 222A, desorptiongas is able to flow through the packed trap 222A while heating continuesto a specified temperature (e.g., a desorption temperature in the rangeof 100-300° C.) and compounds retained by the packed trap 222A are ableto flow toward the polar column 228. One or more polar compounds of thesample can be retained by the polar column 228, while the non-polarcompounds can move on to the PLOT column 222B and separate from eachother after entering the PLOT column 222B, which can fluidly couple tothe polar column 228 via a 3-way valve 226C. Compounds that enter thePLOT column 222B can slow down (flow through the column 222B at a slowerrate than before entering it) and resolve or separate within the PLOTcolumn 222B.

The system 224 may further include a split port (or split vent) 226Adisposed between the polar column 228 and the PLOT column 222B andcapable of fluid communication with the polar column 228 via the 3-wayvalve 226C (e.g., based on the operation of the 3-way valve 226C). Thesplit port 226A can facilitate a process to purge water vapor from thepolar column 228. Relatedly, some embodiments of the disclosure mayinclude a desorption gas valve 226B to selectively flow desorption gasinto one end of the PLOT column 222B to transfer the compounds ofinterest from the PLOT column 222B and toward the second detector 220(i.e., to perform a desorption and detection process at the PLOT column222B).

Thus, the exemplary second trapping system 224 can be used topreconcentrate and perform analysis of one or more sample compounds andto remove water vapor and bulk gases from the system. For example, thesplit port 226A can fluidly couple with the polar column 228 (e.g., byopening the 3-way valve 226C between the two and closing the 3-way valve226C at the PLOT column 222B) after the non-polar C2 hydrocarbons havecompletely or substantially passed through the polar column 228 to thePLOT column 222B (or, in some embodiments, have been further transferredto the second detector 220). The polar column 228 can then be heatedslightly to a flush temperature between 40° C. and 60° C. while fluidlycoupled to the split port 226A to substantially or fully purge watervapor from the polar column 228. The polar column 228 is able to retainFormaldehyde when heated to a temperature in the range of 40° C. to 60°C., thus allowing the water vapor to be purged from the system 224without loss of the ability to detect Formaldehyde in the chemicalsample. As described in greater detail with reference to FIG. 3 below,after water removal, the system 200 can restore fluid communicationbetween the polar column 228 and the PLOT column 222B by turning (i.e.,toggling) the 3-way valve 226C to enable the system 200 to transfer thepolar compounds (e.g., Formaldehyde) from the polar column 228 to thePLOT column 222B (i.e., to retain the remaining polar compounds with theC2 Hydrocarbons on the PLOT column 222B) before a desorption processes(transfer), detection and analysis of all compounds on (or presentwithin) the PLOT column 222B. In some examples of the system 200, the C2hydrocarbons separate as they pass through the PLOT column 222B (e.g.,Acetylene, Ethylene, and Ethane pass through at different rates). Afterthe system 200 transfers the remaining polar compounds (e.g.,Formaldehyde) to the PLOT column 222B, the system 200 can pre-heat thePLOT column 222B with substantially no flow occurring through the PLOTcolumn 222B until after it is heated to a desorb temperature. Once thePLOT column 222B is heated to a desorb temperature, the system 200 canopen the Desorb Gas valve 226B to flow desorb gas to rapidly (i.e.,according to the manner of the flow from desorb gas valve 226B) deliverthe completely separated C2 Hydrocarbons and Formaldehyde to the one ormore second detector(s) 220. The rapid transfer of both C2 hydrocarbonsand Formaldehyde can increase the concentration of each compound in thesecond detector(s) 220 (i.e., to increase the resulting signalintensity), but can also reduce the peak width to produce very narrowpeaks—a goal for most capillary GC systems.

FIG. 2C illustrates an exemplary system 200 for preconcentrating andanalyzing one or more groups of compounds within a chemical sampleaccording to the disclosure. As shown in FIG. 2C, the system 200includes a first trapping system 204 (described in greater detail withreference to FIG. 2A above), a first detector 210 (or first chemicalanalysis device), a second trapping system 224 (described in greaterdetail with reference to FIG. 2B above), one or more second detector(s)220 (or second chemical analysis device) including a packed trap 222A, aswitching valve 240, a pressure control system 244, an polar column 228,a split port 226A, a desorption gas valve 226B, a 3-way valve 226C and aPLOT column 222B. The system 200 can further include one or moreprocessors (e.g., controllers, microprocessors, computers, computersystems, etc.) (not shown) running software and/or instructions housedon a non-transitory computer-readable medium for controlling theoperation of one or more components of the system 200. Moreover, as canbe appreciated by one skilled in the art, the system 200 may include oneor more processors configured to control the operation of certaincomponents within system 200, such as the valve system 240, the 3-wayvalve 226C and the desorption gas valve 226B, along with any othercomponent of the system 200.

As shown in the figures, the system 200 includes a multi-channel streamselect valve 202 to select between various fluid inputs to flow into thesystem 200 (e.g., into one end of the first trap 212 of the firsttrapping system 204). The inputs include an internal standard 202A, afirst calibration standard 202B, a second calibration standard 202C, ablank gas 202D, a first real time sample 202E, and a second real timesample 202F. Additional or alternate inputs are possible. An integratedsample refers to air collected into a vacuum canister over the entireduration of a user-defined integration period, although other samplingtechniques are possible without departing from the scope of thedisclosure. An integrated sample can be input into the system 200 bydrawing approximately 100-500 cc of air from a sample container into thefirst trapping system 204. Other examples of time-integrated samples aredescribed above with reference to FIG. 1 .

Operation of the system 200 can begin with allowing the internalstandard 202A gas channel to flow into the first trapping system 204 viathe multi-channel valve 202 followed by either one of the calibrationstandards 202B, 202C (e.g., to calibrate system 200) or-by selecting atthe multi-channel valve 202 either the first real time sample 202E orthe second real time sample 202F (e.g., a sample or chemical sample) orfrom an autosampler holding sample containers collected remotely (notshown). The first trap 212 of the first trapping system 204 can retainone group of compounds (e.g., C3-C12 hydrocarbons) while fixed gasses(e.g., Nitrogen, Oxygen, Argon, CO2, Methane) and other compounds (e.g.,water vapor, C2 hydrocarbons, Formaldehyde, and light freons boilingbelow −50° C.) pass through the first trap 212 without beingsubstantially retained within the first trap 212.

The compounds that are not retained by the first trap 212 can flowthrough a switching valve (or valve system) 240 and then through thepacked trap 222A of the second trapping system 224 that can be fluidlycoupled to the first trap 212 of the first trapping system 204. Thepacked trap 222A can be packed with a strong adsorbent such as CarbonMolecular Sieve that can retain the compounds (e.g., Formaldehyde, C2hydrocarbons, and water vapor) not retained by the multi-capillarycolumn trap 212 in the first trapping system 204. For example, thepacked trap 222A of the second trapping system 224 can be strong enough(i.e., possessing sufficient chemical affinity based on the column'slength, inner diameter, and/or internal adsorbent coating) to retain thecompounds of interest (e.g., C2 hydrocarbons and Formaldehyde) duringthe preconcentration of 100 cc to 500 cc of air at approximately 35° C.

The volume of gas being trapped by the system 200 illustrated in FIG. 2Ccan be measured by one of several volume measurement techniques employedby today's trapping systems (e.g., mass flow controllers, pressureincrease in a reservoir of known volume, and the like). As shown in FIG.2C, the system can include volume/pressure controllers 242 for thispurpose. In some examples, the volume of gas being measured (e.g., byvolume/pressure controller 242) can constitute the volume of thechemicals not being trapped by either the first trap 212 or the packedtrap 222A, which includes the fixed gases (e.g., N2, O2, Ar, Methane,and some to most of the CO2 and H2O), and, when performing traceanalysis, can often represent 98-99% of a sample. So, the impact onaccuracy of volume measurements from collecting part of a sample (e.g.,any compounds retained by the first trap 212 or the packed trap 222A)before volume measurement (e.g., by volume controller 242) can, in manyembodiments, be negligible.

After trapping the C3 hydrocarbons and heavier compounds within thefirst trap 212 of the first trapping system 204, an inert gas (e.g.,Helium) can be introduced through the multi-channel select valve 202 topurge any remaining air and water out of the first trap 212 of the firsttrapping system 204, while also purging the air and, in someembodiments, can also purge some water vapor from the packed trap 222Aof the second trapping system 224. The first trap 212 of the firsttrapping system 204 can be heated and back flushed towards the secondtrap 232 with a comparatively smaller volume of gas than the volume ofgas passed through the trap 212 during the initial operation (i.e.,first adsorption process) of the first trapping system 204. That is, thevolume of gas passed through the first trap 212 to “focus” the C3hydrocarbons and other, heavier, compounds onto the second trap 232 ofthe first trapping system 204 to allow them to inject more rapidly intothe GCMS column 236. The second trap 232 can then be pre-heated (e.g.,to a desorption temperature in the range of 100-300° C.) under no flowconditions (e.g., without a substantial volume of gas flowing throughthe second trap 232) to facilitate a faster injection rate when thecarrier gas is used to back-flush the second trap 232 to deliver thecompounds that the second trap 232 retains (e.g., C3-C12 hydrocarbons)to the first detector 210 (or first chemical analysis device).

Concurrently or separately from the preheating and injection of thesecond trap 232 (or focusing trap) of the first trapping system 204 intothe chemical separation column 236, the packed trap 222A of the secondtrapping system 224 can also be pre-heated to allow a faster injectionfrom the packed trap 222A into the polar column 228, and can operatewithin separate GC ovens or within separate column mandrels with theirassociated heaters in close proximity to the chemical separation column236. After heating the packed trap 222A, the valve system 240 can rotateto a second state and facilitate a back-flushing process of thecompounds retained in column 222A (e.g., C2 hydrocarbons, Formaldehyde,and any remaining water vapor) from column 222A to the polar column 228.In some examples of system 200, a forward flush of the packed trap 222Acan cause packed trap 222A to act as a separation column and furtherseparate the C2 Hydrocarbons from each other (i.e., in addition to anyseparation of the C2 hydrocarbons and Formaldehyde that can occur in thePLOT column 222B). So, for some examples of the system 200, a forwardflush process of the packed trap 222A can be an advantageous method oftransferring the compounds retained by packed trap 222A (e.g., C2hydrocarbons, Formaldehyde, and any remaining water) to the polar column228 and the PLOT column 222B. For example, a forward flush process ofpacked trap 222A can include switching the two lines connecting to valve240 at ports 3 and 4 with each other (FIGS. 2B and 2C). And in examplesof the system 200 that include a forward flush of the packed trap 222Amay even further separate the C2 Hydrocarbons and Formaldehyde at theSecond Detector(s) 220 (i.e., beyond the separation that would otherwiseoccur in the PLOT column 222B alone).

The polar column 228 can be a polar “ionic liquid” column that retainspolar compounds more readily than non-polar compounds. Thus, any C2hydrocarbons that are flushed into the polar column 228 from the packedtrap 222A can pass through the polar column 228 because they arenon-polar. In some embodiments, the non-polar compounds (e.g., C2hydrocarbons) rapidly flow through the polar column 228 (i.e., based onthe rate of flow through the polar column 228 and the polar column's lowaffinity for non-polar compounds) and to the PLOT column 222B. In otherwords, the back-flushing of the packed trap 222A can facilitate thetransfer of any C2 hydrocarbons initially retained by the packed trap222A through the polar column 228 and, via the 3-way valve 226C, intothe PLOT column 222B while it is at a first temperature (e.g., 30-40°C.), as described above in greater detail with reference to FIG. 2B.

The flow of gas through the polar column 228 can be to the split port226A and can flush, or purge, substantial amounts of water vapor fromthe polar column 228 without purging out the retained Formaldehyde. Thatis, the polar column 228 in system 200 can retain Formaldehyde attemperatures between 40-60° C.; yet, at the same range of temperatures,allows 95%-99% or more of the water vapor initially retained by thecolumn 228 to be eliminated through split port 226A.

After the process to purge water vapor via split port (or split vent)226A (i.e., and the 3-way valve 226C closes at the split port 226A), oneor more heaters can heat the polar column 228 to facilitate the releaseand flow of the Formaldehyde from the polar column 228 to the PLOTcolumn 222B (e.g., by opening the 3-way valve 226C between the polarcolumn 228 and the PLOT column 222B and then flowing gas from theselector valve 240 and through the columns 228, 222B). The system 200can then substantially cease the flow of gas through the PLOT column222B to allow pre-heating of the PLOT column 222B to facilitate a rapidinjection of compounds from the PLOT column 222B (e.g., C2 hydrocarbonsand Formaldehyde) once the flow from the (pre-heated) PLOT column 222Bto the second detector(s) 220 resumes (e.g., by opening desorption gasvalve 226B). That is, heating the PLOT column 222B soon beforedesorption and transfer to the one or more second detector(s) 220 fordetection can reduce signal-peak width, and increase overallsensitivity, of the one or more second detector(s) 220.

After the C2 hydrocarbons have separated from one another and before thecompounds elute through the PLOT column 222B to be detected by the oneor more second detector(s) 220, the flow of fluid through the PLOTcolumn 222B can be stopped. After water elimination and after adding theFormaldehyde to the PLOT column 222B, the PLOT column 222B can then bepre-heated to the desorption temperature (e.g., 100-300° C.) to reduceits affinity for the already separated C2 hydrocarbons and Formaldehyde.The system 200 can open desorption gas valve 226B to cause carrier(desorption) gas to flow into the PLOT column 222B and can flush thecompounds of interest (e.g., Acetylene, Ethylene, Ethane, andFormaldehyde) from the PLOT column 222B to the second detector(s) 220 ata substantially high flow rate. For example, the flow rate of gasthrough the PLOT column 222B can result in reduced peak widths at theone or more second detector(s) 220 of approximately 2-3 seconds.

After injecting the C3 hydrocarbons and heavier compounds (e.g.,compounds having boiling points in the range of −50° C. to 250° C.) intothe chemical separation column 236 and the first detector 210, and theother compounds into the second detector(s) 220, a process to bake outall traps in the system 200 can begin. During bake out, the system 200can be heated to a bake out temperature in the range of 150-230° C. toremove any traces of chemicals remaining in the system 200. Followingthe bake out process the system 200 can cool, e.g., via fans 216A and236B and/or additional or alternate fans, and the system 200 can then beready to trap and analyze the next sample according to the same stepsand overall operation described above.

A computer interface can maintain and control the timing of the system200, together with the operation of its individual components. Forexample, a computer interface can control the concentration of a sampleand can be synchronized with the operation of one or more vacuumcanisters and over a user-defined integration period (e.g., to allow thesystem 200 to operate, for example, every hour, every other hour, every3^(rd) hour, etc.).

FIG. 3 illustrates an exemplary process 300 for analyzing a chemicalsample according to the disclosure. In some embodiments, one or moreprocessors (e.g., controllers, microprocessors, computers, computersystems, etc.) running software and/or instructions housed on anon-transitory computer-readable medium can be used to perform orfacilitate one or more steps of the process 300.

In step 302 of process 300, the sample (e.g., a volume of air) can bedelivered to the first trapping system 204 of system 200. In someembodiments, before delivering the sample to the system 200, acalibration standard (e.g., calibration standard 1 202A or calibrationstandard 2 202B described in detail above with reference to FIG. 2C) canbe delivered to the system 200 (not shown). Moreover, an internalstandard can be added to the system 200 (not shown). Alternatively,during system calibration, the internal standard and one or morecalibration standards can be delivered to the system 200. The sample canbe a real time sample, such as real time sample 202E or real time sample202F. Or it can be from a non-real time sampling container as directlyconnected to the system 200, or through a multi-sample autosampler 2-50or more sample containers for high productivity analysis. Thecalibration standards, samples, and other gases such as internalstandards or blanks can be coupled to the system by an autosampleroperatively coupled to the stream select valve 202. Generally, theautosamplers can add additional sample capacity. The internalstandard(s) and calibration standards can directly connect to the system200 through the inlet valve 202. Thus, the sample can enter the firsttrap 212 of the first trapping system 200. As described above withreference to FIGS. 2A-C, the first trap 212 of the first trapping system204 can be a Multi-Capillary Column Trapping System (MCCTS) consistingof a series of multiple capillary columns of increasing retentionstrength from weakest to strongest.

In step 304 of process 300, the first trapping system 204, the firsttrap 212 of the first trapping system can trap the heavier (e.g., C3hydrocarbons and above) compounds of the sample. During step 304, thefirst trap 212 of the first trapping system 204 can be at a trappingtemperature that is in the range of 30-40° C. (e.g., 35° C.), which cancause the sample compounds to be retained in the first trap 212.

In step 306 of process 300, the lighter sample compounds (e.g., C2hydrocarbons and Formaldehyde), bulk gases, and water vapor can traversethe first trap 212 of the first trapping system 204 and enter the packedtrap 222A of the second trapping system 224. As described above withreference to FIGS. 2A-C, the packed trap 222A of the second trappingsystem 224 can be a packed trap containing a strong adsorbent to retainC2 Hydrocarbons and Formaldehyde that were not trapped by the first trap212 of the first trapping system 204.

Thus, steps 302-306 of process 300 can separate the heavier compounds(e.g., C3 hydrocarbons and heavier) from the lighter compounds (e.g., C2hydrocarbons and Formaldehyde). The heavier compounds can be trappedusing the first trapping system 204 while the lighter compounds can passthrough the first trapping system 204. Additionally, and as described ingreater detail above with reference to FIG. 2B, the second trappingsystem 224 can receive the light compounds from the first trappingsystem 204 and can remove the water vapor from the light compounds(e.g., C2 hydrocarbons and Formaldehyde) and eventually transfer them toone or more second detector(s) 220 for chemical analysis. Theseprocesses can be executed at the same time or in series.

In step 308 of process 300, the first trap 212 of the first trappingsystem 204 can be heated to a desorption temperature (e.g., 100-300°C.), thereby reducing the affinity of the one or more trapped compoundsto the trap 212.

In step 310 of process 300, the first trap 212 of the first trappingsystem 204 can be back-flushed to the second trap 232 of the firsttrapping system 204. As described above with reference to FIGS. 2A-2C,the second trap 232 of the first trapping system can further focus thesample into a smaller volume. Focusing the sample in this way canimprove the signal to noise ratio and improve chromatographic resolutionof the chemical analysis results by increasing peak height and reducingpeak width, respectively.

In step 312 of process 300, the second trap 232 of the first trappingsystem 204 can be heated to a desorption temperature (e.g., 100-300°C.), thereby reducing the affinity of the one or more trapped compoundsto trap 232.

In step 314 of process 300, the second trap 232 of the first trappingsystem 204 can be back-flushed to the first detector 210. The compoundscan traverse a chemical separation column 236 (e.g., a GC column) beforeentering the detector (e.g., an MS).

In step 315 of process 300, the one or more heavier compounds (e.g., C3hydrocarbons and heavier) can undergo chemical analysis using the firstdetector 210.

Thus, steps 308-315 of process 300 can be used to focus and analyze oneor more heavier compounds, such as C3 hydrocarbons and heavier, of thechemical sample. During, before, or after steps 308-315, the process 300can proceed to steps 316-344.

In step 317 of process 300, the 3-way valve 226C can open between thepolar column 228 and the PLOT column 222B and the 3-way valve 226C canclose between the polar column 228 and the split port 226A. Operatingthe 3-way valve in this way fluidly couples the polar column 228 and thePLOT column 222B while closing the split port 226A, which can allow oneor more compounds to flow through the polar column 228 to the PLOTcolumn 222B without exiting the system through the split port 226A, aswill be described below.

In step 316 of process 300, the packed trap 222A of the second trappingsystem 224 containing the C2 hydrocarbons, Formaldehyde, and water vaporcan be heated to a desorption temperature (e.g., 100-300° C.) inpreparation for transferring these compounds to the rest of the secondtrapping system 224.

In step 318 of process 300, the valve system 240 can be thrown to itsalternate position to allow the flow through the packed trap 222A of thesecond trapping system 224 to be reversed.

In step 320 of process 300, the packed trap 222A of the second trappingsystem 224 can be back-flushed (e.g., using high purity pressurecontrolled helium 244). That is, the flow through the packed trap 222Acan proceed in the opposite direction of the direction of flow when thecompounds entered the packed trap 222A towards the polar column 228 andPLOT column 222B. In some examples, and as described above, the system200 can use the packed trap 222A similar to a packed column and forwardflush the packed trap 222A towards the polar column 228 and PLOT column222B, and may thereby separate compounds retained by the packed trap222A (e.g., C2 Hydrocarbons and Formaldehyde) before the compounds reachthe polar column 228 and the PLOT column 222B (where the compounds cancontinue to separate). In step 322 of process 300, one or more polarcompounds of the sample (e.g., Formaldehyde and water vapor) can beretained by the polar column 228.

In step 324 of process 300, one or more non-polar compounds of thesample (e.g., C2 hydrocarbons) can flow through the polar column 228 andbe retained and separated (or further separated) by the PLOT column222B. Steps 322-324 can occur fully or partially at the same time.

Thus, steps 316-324 can separate the polar and non-polar components ofthe sample not retained by the first trap 212 of the first trappingsystem 204. The non-polar compounds, such as the C2 hydrocarbons, can befocused and separated by the PLOT column 222B while the polar compounds,such as water vapor and Formaldehyde, can be retained by the polarcolumn 228.

In step 326 of process 300 the system 200 (or, in some embodiments, thesecond trapping system 224) can close the 3-way valve 226C between thepolar column 228 and the PLOT column 222B and the 3-way valve 226C canopen between the polar column 228 and the split port 226A.

In step 328 of process 300 the system 200 can heat the polar column 228to a flush temperature, or a water transfer temperature, between 40° C.and 60° C. Heating the polar column 228 to a flush or water transfertemperature can facilitate eliminating water from the polar column 228through the split port 226A without eliminating compounds of interest(e.g., Formaldehyde), as described above with reference to FIGS. 2B-C.

In step 330 of process 300 the system 200 can transfer any waterretained by the polar column 228 to the split port 226A. That is, anywater vapor retained on the polar column 228 can be pushed out of thesecond trapping system 224 (and, more generally, the system 200) throughsplit port 226A via the 3-way valve 226C. This can be accomplished byfacilitating a flow of carrier fluid through the polar column 228 (whilethe polar column 228 is heated to the water transfer temperature between40° C. and 60° C.) towards the split port 226A. Because the elutionvolume of Formaldehyde is much greater than that of water at 40-60° C.the Formaldehyde can remain on the polar column 228 during step 330.

In step 332 of process 300 the system 200 can close the 3-way valve 226Cat the split port 226A.

In step 334 of process 300 the system 200 can heat the polar column 228to a desorption temperature between 100-300° C. Moreover, in manyembodiments of system 200, during pre-heating step 334 the system 200substantially prevents flow through the polar column 228 (e.g., “noflow” condition) to enable rapid transfer of compounds from the polarcolumn 228 to the PLOT column 222B once flow through the polar column228 begins after the pre-heating step 334.

In step 336 of process 300 the system 200 can open the 3-way valve 226Cbetween the polar column 228 and the PLOT column 222B.

In step 338 of process 300, any remaining polar compounds (e.g.,Formaldehyde) can be transferred from the polar column 228 to the PLOTcolumn 222B. During step 338, the PLOT column 222B can be at a trappingtemperature in the range of 30-40° C. (e.g., 35° C.) and gas can flowthrough the polar column 228 to the PLOT column 222B. Thus, theremaining polar compounds (e.g., Formaldehyde) can be transferred to,and retained by, the PLOT column 222B.

In step 340 of process 300 the system 200 (or in some embodiments, thesecond trapping system 224) can close the 3-way valve 226C between thepolar column 228 and the PLOT column 222B. For example, the system 200can control the 3-way valve 226C based on a volume transferred from thepolar column 228 to the PLOT column 222B. And in many embodiments, thesystem 200 can transfer Formaldehyde to the PLOT column 222B from thepolar column 228 in a sufficiently small volume (e.g., using a transferprocesses of sufficiently small volume) to prevent, or reduce, the C2hydrocarbons from prematurely eluting to the second detector(s) 220,such as before the final PLOT column 222B desorb stage (i.e., step 346of process 300 described below).

In step 342 of process 300 the system 200 can perform a pre-heatingprocess for the PLOT column 222B (i.e., pre-heat the PLOT column 222B toa desorption temperature between 100-300° C.). For example, in someembodiments, one or more heaters (e.g., heating wire, GC oven, mandrelheater, etc.) can pre-heat the PLOT column 222B before thedesorption/detection step to facilitate injection of all compoundsretained and separated by the PLOT column 222B (e.g., C2 hydrocarbonsand Formaldehyde). And at this desorption temperature, the affinity ofthe C2 hydrocarbons and Formaldehyde to the PLOT column 222B candecrease, which can allow the C2 hydrocarbons and Formaldehyde to berapidly injected into the second detector(s) 220, as will be describedbelow. The flow of fluid into, or out of, the PLOT column 222B can ceaseuntil the system 200 begins to transfer the compounds to the seconddetector(s) 220 during a desorption step. That is, system 200 canperform step 342 of process 300 with substantially no flow through PLOTcolumn 222B. The system 200 is able to reduce, substantially reduce, orprevent the flow of gas through the PLOT column 222B by ceasing to flowgas into the various inputs of the system 200, or by closing a valve atone end of the column 222B. For example, closing the 3-way valve at thePLOT column 222B and closing desorption gas valve 226B can prevent theflow of gas to the PLOT column 222B, such as during a pre-heatingprocess described above.

In step 344 of process 300 the system 200 can open desorption gas valve226B to facilitate the flow of desorb gas into the PLOT column 222B.

In step 346 of process 300 the system 200 (or the second trapping system224) can perform a desorption process to transfer the compoundsinitially retained by the PLOT column (e.g., C2 hydrocarbons andFormaldehyde) to the second detector(s) 220 and perform a chemicalanalysis of those compounds. The system 200 can resume flow of gas into(and thus out of) the PLOT column 222B by opening desorption gas valve226B (as described with reference to step 346 above) and, as a result,cause the compounds retained on the PLOT column 222B to flow rapidly tothe second detector(s) 220.

The system 200 (using the one or more second detectors 220) can analyzethe compounds transferred from the PLOT column 222B to the seconddetector(s) 220. For example, the second detector(s) 220 can be one ormore of a photoionization detector and/or a flame ionization detector,as described in greater detail with reference to FIG. 2B above.Additionally, in some embodiments, the system 200 can analyze the signalgenerated by the second detector(s) 220 during steps 315 and 346. Morespecifically, one of more computer systems can interact with (or beincluded in) system 200 and can determine a width of a signal-peakgenerated during step(s) 315 or 346 in seconds (e.g., between 2-3seconds for some embodiments) and can determine a relative magnitudebetween one or more peaks generated during embodiments of process 300performed by system 200. As can be appreciated, the system 200 candetermine an amount of each compound based on the area of each peak(e.g., the system 200 can integrate one or more peaks with electronics,one or more computer systems, one or more microprocessors, or the like).Moreover, the system 200 (or a microprocessor of the system 200) canmultiply the area counts by a response factor. In some examples, thesystem can determine one or more response factors based on a calibrationprocess performed by system 200 with a sample of known concentrations(standard) input to the system 200. Alternatively or in addition, one ormore response factors can be predetermined and given to the system 200.And as can also be appreciated, the system 200 can adjust one or moreresponse factors based on the response of a co-injected (concurrentlyinput) internal standard of the system 200.

In step 348 of process 300 or after chemical analysis has been performedon all compounds of the sample (e.g., steps 315 and 346 of process 300),the system 200 can be baked out and then cooled to the initial trappingtemperature in preparation for the next run. The system can be heated totemperatures in the range of 100-300° C. during bake out to remove anycompounds remaining within the system 200, thereby cleaning the system200 for the next run. Following bake out, the system 200 can be returnedto the initial trapping temperature in the range of 30-40° C. (e.g., 35°C.) to allow trapping of the compounds of the next sample.

FIG. 4 illustrates an exemplary system 400 for preconcentrating andanalyzing one or more groups of compounds within a chemical sampleaccording to the disclosure. System 400 can include the same or similarcomponents as system 200 described above with reference to FIG. 2C,except as otherwise illustrated and described. System 400 includesultralight compound trap 422A, focusing column 422B, and separationcolumn 422C.

In some examples, system 400 can analyze both the heavier compounds inthe C3-C12 volatility range and the lighter C2 hydrocarbons andformaldehyde using one detector 410 (e.g., a mass spectrometer). Inembodiments using one detector 410 to analyze both the ultralightcompound and the heavier compounds, the ultralight compounds can betransferred to the detector 410 via the second trap 432 of the firsttrapping system 404 and the GC column 436, both of which act as atransfer line for the ultralight compounds. That is to say, theultralight compounds have such a low affinity for the second trap 432 ofthe first trapping system 404 and the GC column 436 that they do notundergo further separation and/or band-broadening while traversing thesestages on their way to the detector 410. Instead, the ultralightcompounds can be trapped, focused, and split by the second trappingsystem 424, as will be described in more detail with reference to FIGS.4 and 5 . In some examples, however, system 400 can include a seconddetector (e.g., an ARC detector) at the outlet of the separation column422C to analyze the ultralight compounds and can use detector 410 toanalyze the heavier compounds (e.g., C3 and heavier).

To facilitate flow of the compounds during preconcentration, system 400includes a number of volumetric flow controllers, such as controller442, 444, and 452. In some embodiments, one volumetric flow controlleraccesses the system 400 at one or more of the points indicated by 442,444, and 452.

System 400 includes a first trapping system 404 and a second trappingsystem 424. The first trapping system 404 includes the same componentsas the first trapping system 204, but operates differently, as will bedescribed in further detail below, in that the light compounds can beintroduced to the second trap 432 of the second trapping system 404 viainlet 436 after separation of C2 hydrocarbons from formaldehyde andremoval of water vapor and other bulk gases, as will be described below.The second trapping system 424 includes many of the same components ofsecond trapping system 224 with some different components noted herein,but may not include a second detector, as the light compounds can beanalyzed by the same detector 410 that analyzes the heavier compounds.

In a manner similar to that described above with reference to FIGS. 1-3, a sample 402E or 402F including ultralight (e.g., C2 hydrocarbons(Ethane, Ethylene, Acetylene) and formaldehyde) compounds and heaviercompounds (e.g., C3 hydrocarbons and heavier) can be introduced into thefirst trap 412 of the first trapping system 404 through sample source402. The heavier compounds can be retained by the first trap 412 whilethe lighter compounds, bulk gases, and water vapor can traverse thefirst trap 412 of the first trapping system 404 and enter ultralightcompound trap 422A. Thus, the heavy compounds and ultralight compoundscan be collected in separate traps. Ultralight compound trap 422A can bea packed trap having a length in the range of 2 to 5 feet and an outerdiameter of 1/16 inches to ¼ inches.

The second trapping system 424 is able to remove bulk gases andsubstantially remove water vapor from the sample. While the valve system440 is in the configuration illustrated in FIG. 4 , a portion of watervapor (e.g., 90-95% of the water vapor included in the sample) is ableto traverse the ultralight compound trap 422A to be removed from thesystem by the sample volume measurement and flow controller 442/452during dry purging of the ultralight compound trap 422A. Once all of theultralight compounds have transferred from the first trap 412 of thefirst trapping system 404 and a significant portion (e.g., 90-95%) ofthe water vapor and most of the air (e.g., about 99%) has been removedfrom the system 400, the valve system 440 is thrown into an alternateposition that connects the ultralight compound trap 422A to the focusingcolumn 422B via valve positions 5 and 4. The valve system 440 can bethrown before one or more ultralight compounds of interest (e.g.,acetylene) are able to traverse the ultralight compound trap 422A andexit the system. Thus, in some embodiments, water vapor is removed fromthe system 400 and the compounds of interest are retained by ultralightcompound trap 422A. In order to facilitate separation of water vaporfrom the ultralight compounds of interest, ultralight compound trap 422Acan have a length in the range of 2 to 5 feet in some embodiments. Afterthe ultralight compound trap 422A has been dry purged to remove thewater vapor and air, the ultralight compound trap 422A can then beheated to a desorption temperature and desorbed towards focusing column422B.

Focusing column 422B can be a PLOT column having a length in the rangeof 5 to 50 meters and an inner diameter in the range of 0.25 to 0.53 mm.Transferring the ultralight compounds to the focusing column 422B canreduce the volume of the sample to enable separation of the variousultralight compounds. While the ultralight compounds are retained by thefocusing column 422B, the focusing column 422B can be preheated underno-flow conditions and then the compounds can be transferred to theseparation column 422C. Valve system 440 can be in the configurationillustrated in FIG. 4 during transfer of the compounds from the focusingcolumn 422B to the separation column 422C.

The separation column 422C can be a PLOT column (e.g., carbon molecularsieve PLOT column or Carboxen PLOT column) having a length in the rangeof 5 to 20 meters and an inner diameter in the range of 0.25 to 0.53 mm.In some embodiments, the remaining water vapor, air, and bulk gases inthe sample are able to traverse focusing column 422B and separationcolumn 422C more readily than the ultralight compounds of interest.Thus, the water vapor, air, and bulk gases that were not removed by drypurging the ultralight compound trap 422A can be removed by controller452 while the compounds of interest are trapped on the separation column422C. Additionally, transferring the ultralight compounds from thefocusing column 422B to the separation column 422B can separate thecompounds into separate peaks for detection by detector 410. In someembodiments, separating the compounds with focusing column 422B and/orseparation column 422C can be advantageous, as the GC column 436 may notbe strong enough to separate the ultralight compounds without the use ofcryogenic cooling.

Once the water vapor, bulk gases, and air have been removed and whilethe ultralight compound are trapped by the separation column 422C, theseparation column 422C can be heated to a desorption temperature and acarrier gas source 426B can provide a carrier gas to desorb thecompounds from the separation column 422C, with the flow beingcontrolled by a fixed restrictor. Due to the consistent pressure of thecarrier gas source 426B, the rate of transfer can be reproducable.

In some embodiments, instead of analyzing the ultralight compounds witha separate detector as described above with reference to FIGS. 1-3 ,system 400 can transfer the ultralight compounds from the separationcolumn 422C to the second trap 432 of the first trapping system 404 andanalyze the ultralight compounds using detector 410. Before theultralight compounds reach the second trap 432 of the first trappingsystem 404, the heavier compounds can be transferred from the first trap412 of the first trapping system 404 to the second trap 432 of the firsttrapping system, with the second trap 432 being at a trappingtemperature in the range of 30-40° C. when the heavier compounds aretransferred from the first trap 412 and the ultralight compounds aretransferred from the separation column 422C. While all compounds areretained by the second trap 432, the second trap 432 can be pre-heatedto a desorption temperature. The ultralight compounds can remainseparated from one another and traverse the second trap 432 withoutbeing subject to band-broadening. Next, the compounds (e.g., both theultralight compounds and the heavier compounds) can traverse the secondtrap 432 and elute to the GC column 436. The ultralight compounds areable to traverse the second trap 432 and GC column 436 more readily thanthe heavier compounds and can remain separated in the manner achieved bythe focusing column 422B and separation column 422C describedpreviously. All compounds (e.g., heavier compounds and ultralightcompounds) can be analyzed by detector 410 (e.g., a mass spectrometer).The GC column 436 separates the heavier compounds before analysis bydetector 410 (e.g., a mass spectrometer).

In a manner similar to the manner described above with respect to FIGS.1-3 , the heavier compounds can be focused by the first trapping system404 before being analyzed by detector 410. Analyzing both the heaviercompounds and the ultralight compounds with detector 410 enables system400 to deliver the chemical analysis results in one chromatogram. Afteranalysis is complete, the system 400 can be heated to the desorptiontemperature and backflushed to remove any compounds not removed from thesystem or transferred to the detector 410. During backflushing, whilerotary valve 440 is in the position illustrated in FIG. 4 , valve 428can be opened and bakeout gas 454 can be introduced into the secondtrapping system 424 by controllers 442, 444 and/or 452 to remove anyremaining compounds from the focusing column 422B and separation column422C.

In some embodiments, rather than transferring the ultralight compoundsfrom the separation column 422C, the ultralight compounds can beanalyzed using a second detector separate from detector 410. Forexample, a mass spectrometer can be used as detector 410 and anadditional detector, such as an ARC detector, which has good sensitivityfor the ultralight compounds, can be fluidly coupled to the outlet ofseparation column 422C to analyze the ultralight compounds. The variousultralight compounds can be separated prior to detection by the focusingcolumn 422B and separation column 422C as described above.

FIG. 5 illustrates an exemplary process 500 for analyzing a chemicalsample according to the disclosure. Several steps of process 500 can bethe same or similar to several steps of process 300, described abovewith reference to FIG. 3 .

For example, steps 502-506 of process 500 can be similar to steps302-306 of process 300. In steps 502-506, the heavier compounds (e.g.,C3 hydrocarbons and heavier) can be separated from the ultralightcompounds (e.g., C2 hydrocarbons and formaldehyde). The heaviercompounds can be trapped using the first trapping system 404 while theultralight compounds can pass through the first trapping system 404. Theultralight compounds can be trapped by ultralight compound trap 422A.

At step 507, the ultralight compound trap 422A can be dry purged. Duringthis process, a substantial portion (e.g., 90-95%) of water vapor andmost (e.g., 99%) of the air in the sample can be removed from thesystem. The ultralight compounds can remain trapped by ultralightcompound trap 422A.

After the ultralight compounds have been removed from the first trappingsystem 404, the first trap 412 of the first trapping system 404 can bepreheated to a desorption temperature at step 508.

At step 510, the first trap 412 of the first trapping system 404 can bebackflushed to transfer the heavier compounds to the second trap 432 ofthe first trapping system 404.

Before, during, or after steps 508 and 510, steps 516-532 can beperformed to focus and separate the ultralight compounds of the sample.At step 516, the ultralight compound trap 422A can be preheated underno-flow conditions to a desorption temperature.

At step 518, the valve system 440 can be thrown into its alternateconfiguration, which couples the ultralight compound trap 422A to thefocusing column 422B.

At step 520, the ultralight compound trap 422A can be backflushed.Backflushing the ultralight compound trap 422A can introduce a flow in adirection from the ultralight compound trap 422A to the focusing column422B. This flow can transfer the ultralight compounds from theultralight compound trap 422A to the focusing column 422B. Transferringthe ultralight compounds to the focusing column 422B reduces the volumeof the sample, thereby focusing it.

At step 521, the focusing column 422B can be preheated to a desorptiontemperature and at step 522, the compounds can be transferred from thefocusing column 422B to the separation column 422C. During this transferprocess, the valve system 440 can be in the configuration illustrated inFIG. 4 and flow can be controlled by controller 444. Transferring thecompounds from the focusing column 422B to the separation column 422Ccan cause the various ultralight compounds to separate from one another.This separation can be maintained for the duration of process 500.

The transfer of compounds from focusing column 422B to separation column422C can facilitate removal of remaining water vapor and air from thesystem 400. Water vapor and air are able to traverse the focusing column422B and the separation column 422C more readily than the samplecompounds of interest. Thus, while the compounds of interest areretained on one or more of columns 422B and 422C, the air and water canbe removed by flow controller 452.

At step 526, the GC indicates that it is ready. Once the GC is ready,the ultralight compounds can be transferred from the separation column422C to the second trap 432 of the first trapping system 404.

At step 432, the ultralight compounds can be transferred from separatingcolumn 422C to the second trap 432 of the first trapping system 404 bycarrier gas 426B. The ultralight compounds can remain separated from oneanother as they are transferred to the second trap 432 of the firsttrapping system 404 and until they ultimately reach the detector 410, aswill be described in more detail below. The GC column 436 does notfurther separate or band-broaden the ultralight compounds.

As described above, before 516-532, the heavier compounds can betransferred to the second trap 432 of the first trapping system 404 atstep 510. Thus, all of the compounds can be retained by the second trap432 of the first trapping system 404 after the completion of step 510,which can occur while the second trap 432 is at a temperature in therange of 30-40° C.

At step 512, the second trap 432 of the first trapping system 404 can bepreheated to a desorption temperature under no-flow conditions. At step514, the second trap 432 of the first trapping system 404 can bebackflushed to introduce a flow in a direction from the strong column438C to weak column 438A.

Backflushing the second trap 432 after preheating can transfer thetrapped compounds from the second trap 432 to the GC column 436 anddetector 410. As described above with reference to FIG. 4 , theultralight compounds can traverse the second trap 432 of the firsttrapping system 404 faster than the heavier compounds. Moreover, in someembodiments, the ultralight compounds remain separated as they elute tothe GC column 436 and detector 410 and do not separate further orundergo band-broadening. As the heavier compounds elute to the GC column436 and detector 410, they can undergo separation as they traverse theGC column 436, allowing for the peaks of the various compounds to beresolved by detector 410.

At step 515, chemical analysis can be conducted using detector 410. Thedetector 410 can produce a chromatogram including a peak representingeach compound included in the sample.

Thus, both the heavy compounds and the ultralight compounds can beanalyzed by detector 410. In some embodiments, analyzing all of thecompounds in the sample at one detector has the advantage of deliveringall of the analysis data in one chromatogram, instead of providingseparate data sets for each of two detectors. A high-sensitivity massspectrometer can be incorporated into system 400 for use in method 500to detect all of the sample compounds. Analyzing the ultralightcompounds by mass spectrometer is also advantageous because formaldehydeis not detectable using a flame ionization detector (FID). Moreover, Amass spectrometer only needs either Helium or Hydrogen, whereas FIDs andARC detectors require UHP Nitrogen, Hydrogen, and Zero Air (VOC-freeair), which creates more complication and cost, especially when performcontinuous monitoring of VOCs in air.

Once the compounds have been analyzed, step 548 can be used to bake outthe system 400 and then cool the system to the trapping temperature in amanner similar to step 348 of method 300.

In some embodiments, rather than analyzing all compounds using detector410, a second detector can be included at the outlet of the separationcolumn 422C to analyze the ultralight compounds. Instead of transferringthe ultralight compounds from separation column 422C to the second trap432 of the first trapping system 404 at step 532, the ultralightcompounds can elute from the separation column 422C to a seconddetector, such as an ARC detector. Thus, steps 514 and 515 can be usedto transfer the heavier compounds through the GC column 436 to thedetector 410 and conduct analysis on the heavier compounds with detector410.

Therefore, according to the above, some embodiments of the disclosureinclude a system for analyzing a chemical sample, comprising: a firsttrapping system configured to trap one or more first compounds of thechemical sample; a second trapping system comprising a packed trap, apolar column, an output port and a PLOT column, wherein: the polarcolumn is coupled to the PLOT column in series, the second trappingsystem is fluidly coupled to the first trapping system, and the secondtrapping system is configured to trap one or more second compounds ofthe chemical sample and one or more third compounds of the chemicalsample; and one or more valves configured to: during a first trappingprocess: facilitate flow of the chemical sample into a portion of thefirst trapping system in a first direction, wherein the one or morefirst compounds of the chemical sample are trapped in the portion of thefirst trapping system during the first trapping process; and facilitateflow of the one or more second compounds of the chemical sample and theone or more third compounds of the chemical sample through the portionof the first trapping system and to the packed trap of the secondtrapping system, during a first desorption process of the secondtrapping system: facilitate flow of desorption gas through the packedtrap of the second trapping system; transfer the one or more secondcompounds of the chemical sample and water vapor of the chemical sampleto the polar column of the second trapping system; and transfer the oneor more third compounds of the chemical sample through the polar columnof the second trapping system and into the PLOT column of the secondtrapping system, and during a purging process, facilitate flow of thewater vapor from the polar column to the vent port of the secondtrapping system. Additionally or alternatively, in some embodiments, thesystem further includes a chemical separation column fluidly coupled tothe first trapping system and a first detector fluidly coupled in serieswith the chemical separation column. Additionally or alternatively, insome embodiments, the system further includes one or more seconddetectors fluidly coupled to the second trapping system. Additionally oralternatively, in some embodiments, the one or more second detectorscomprise two second detectors fluidly coupled in series to the PLOTcolumn of the second trapping system. Additionally or alternatively, insome embodiments, the one or more first compounds retained within thefirst trapping system are one or more of C3 hydrocarbons or compoundsheavier than C3 hydrocarbons or compounds having higher boiling pointsthan C3 hydrocarbons. Additionally or alternatively, in someembodiments, the one or more second compounds include Formaldehyde.Additionally or alternatively, in some embodiments, the one or morethird compounds are C2 hydrocarbons. Additionally or alternatively, insome embodiments, the one or more third compounds comprise at least oneof Ethane, Ethylene, or Acetylene. Additionally or alternatively, insome embodiments, the one or more valves are further configured to:transfer the one or more second compounds from the polar column to thePLOT column after the purging process, and after transferring the one ormore second compounds to the PLOT column, transfer the one or moresecond compounds and the one or more third compounds from the PLOTcolumn to the one or more second detectors. Additionally oralternatively, in some embodiments, the system further includes one ormore heaters configured to heat the polar column to a purgingtemperature between 40 and 60 degrees Celsius after the one or morethird compounds have been transferred to the PLOT column and before thepurging process, wherein the polar column remains at the purgingtemperature during the purging process. Additionally or alternatively,in some embodiments, the first trapping system comprises: a first trapcomprising a plurality of first capillary columns in series, theplurality of first capillary columns arranged in order of increasingchemical affinity to the one or more first compounds of the sample.Additionally or alternatively, in some embodiments, the first trappingsystem further comprises a second trap, and during a first desorptionprocess of the first trapping system that occurs after the firsttrapping process, the one or more first compounds of the sample flow ina reverse direction from the first trap of the first trapping system tothe second trap of the second trapping system. Additionally oralternatively, in some embodiments, the second trap of the firsttrapping system comprises a plurality of second capillary columns inseries, the plurality of second capillary columns arranged in order ofincreasing chemical affinity to the one or more first compounds of thesample.

Some embodiments of the disclosure are directed to a method comprisingduring a first trapping process: facilitating flow of a chemical sampleinto a portion of a first trapping system in a first direction, whereinone or more first compounds of the chemical sample are trapped in theportion of the first trapping system during the first trapping process;and facilitate flow of one or more second compounds of the chemicalsample and one or more third compounds of the chemical sample throughthe portion of the first trapping system and to a second trapping systemthat is fluidly coupled to the first trapping system, wherein the one ormore second compounds of the chemical sample and the one or more thirdcompounds of the chemical sample are not retained by the first trappingsystem during the first trapping process; during a first desorptionprocess of the second trapping system: facilitating flow of desorptiongas through a packed trap of the second trapping system; transferringthe one or more second compounds of the chemical sample and water vaporof the chemical sample to a polar column of the second trapping system;and transferring the one or more third compounds of the chemical samplethrough the polar column of the second trapping system and into a PLOTcolumn of the second trapping system, the polar column and the PLOTcolumn being connected in series, and during a purging process,facilitating flow of the water vapor from the polar column to an outputport of the second trapping system while the one or more secondcompounds of the sample remain on the polar column. Additionally oralternatively, in some embodiments, the method further comprisesseparating the one or more first compounds of the sample using achemical separation column fluidly coupled to the first trapping system;and performing chemical analysis of the one or more first compounds ofthe sample using a first detector fluidly coupled in series with thechemical separation column. Additionally or alternatively, in someembodiments, the method further includes performing chemical analysis ofthe one or more second compounds of the sample and the one or more thirdcompounds of the sample using one or more second detectors fluidlycoupled to the second trapping system. Additionally or alternatively, insome embodiments, the method further includes transferring the one ormore second compounds from the polar column to the PLOT column after thepurging process, and after transferring the one or more second compoundsto the PLOT column, transferring the one or more second compounds andthe one or more third compounds from the PLOT column to the one or moresecond detectors. Additionally or alternatively, in some embodiments,the method further includes heating, with one or more heaters, the polarcolumn to a purging temperature between 40 and 60 degrees Celsius afterthe one or more third compounds have been transferred to the PLOT columnand before the purging process, wherein the polar column remains at thepurging temperature during the purging process. Additionally oralternatively, in some embodiments, the first trapping system comprises:a first trap comprising a plurality of first capillary columns inseries, the plurality of first capillary columns arranged in order ofincreasing chemical affinity to the one or more first compounds of thesample. Additionally or alternatively, in some embodiments, the firsttrapping system further comprises a second trap, and during a firstdesorption process of the first trapping system that occurs after thefirst trapping process, the one or more first compounds of the sampleflow in a reverse direction from the first trap of the first trappingsystem to the second trap of the second trapping system.

Some examples of the disclosure are directed to a system for analyzing achemical sample including one or more detectors, a first trapping systemconfigured to trap, focus, and separate one or more first compounds ofthe chemical sample, and transfer the one or more first compounds of thechemical sample to one of the one or more detectors for chemicalanalysis, and a second trap configured to trap, focus, and separate oneor more second compounds of the chemical sample, while trapping,focusing, and separating the one or more second compounds of thechemical sample, remove one or more third compounds of the chemicalsample; and transfer the one or more third compounds of the chemicalsample to one of the one or more detectors for chemical analysis,wherein the one or more second compounds and the one or more thirdcompounds traverse at least a portion of the first trapping systembefore entering the second trapping system. Additionally oralternatively, in some examples, the second trapping system comprises anultralight compound trap that is configured to trap the one or moresecond compounds of the sample while allowing the one or more thirdcompounds of the sample to traverse the ultralight compound trap to exitthe system. Additionally or alternatively, in some examples, theultralight compound trap is a packed trap. Additionally oralternatively, in some examples, the second trapping system includes afocusing column configured to trap the one or more second compoundswhile allowing the remaining one or more third compounds to traverse thefocusing trap to exit the system. In some embodiments, the ultralightcompound trap is fluidly coupled to the focusing column. Additionally oralternatively, in some embodiments, the second trapping system furthercomprises a separation column fluidly coupled to the focusing column andtransferring the one or more second compounds from the focusing columnto the separation column causes chemical separation of the one or moresecond compounds. Additionally or alternatively, in some examples, thefocusing column and the separation column are PLOT columns. Additionallyor alternatively, in some examples, the system analyzes the first one ormore compounds of the sample and the second one or more compounds of thesample with a single detector. Additionally or alternatively, in someexamples, the first trapping system comprises a first trap and a secondtrap, the first trap being fluidly coupled to the second trap at a firstend of the first trap and to the second trapping system at a second endof the first trap. Additionally or alternatively, in some examples, thesecond trap of the first trapping system is coupled to the first trap ofthe first trapping system at a first end of the second trap.Additionally or alternatively, in some examples, the one or more secondcompounds are transferred from the separation column of the secondtrapping system to the second trap of the first trapping system at asecond end of the second trapping system and the second one or morecompounds remain separated from one another as they traverse the secondtrap of the first trapping system. Additionally or alternatively, insome examples, the single detector produces one chromatograph indicativeof both the one or more first compounds and the one or more secondcompounds. Additionally or alternatively, in some examples, the systemincludes two detectors. Additionally or alternatively, in some examples,a first detector of the two detectors is fluidly coupled to the firstend of the second trap of the first trapping system and conducts achemical analysis of the one or more first compounds. Additionally oralternatively, in some examples, a second detector of the two detectorsis fluidly coupled to the separation column and analyzes the one or moresecond compounds. Additionally or alternatively, in some examples, theone or more first compounds are compounds in the C3-C12 range.Additionally or alternatively, in some examples, the one or more secondcompounds are C2 hydrocarbons and/or formaldehyde. Additionally oralternatively, in some examples, the one or more third compounds are airand water. Additionally or alternatively, in some examples, stages thattrap compounds trap the compounds at a trapping temperature and desorbthe compounds at a desorption temperature that is higher than thetrapping temperature.

Although examples have been fully described with reference to theaccompanying drawings, it is to be noted that various changes andmodifications will become apparent to those skilled in the art. Suchchanges and modifications are to be understood as being included withinthe scope of examples of this disclosure as defined by the appendedclaims.

The invention claimed is:
 1. A system for analyzing a chemical sample,comprising: one or more detectors; a first trapping system including afirst multi-capillary column trap and a second multi-capillary columntrap, the first trapping system configured to: trap, focus, and separateone or more first compounds of the chemical sample, includingfacilitating a first flow of the one or more first compounds into thefirst multi-capillary column trap of the first trapping system in afirst direction; transfer the one or more first compounds of thechemical sample to one of the one or more detectors for chemicalanalysis without allowing the one or more first compounds to traverse asecond trapping system different from the first trapping systemincluding facilitating a second flow of the one or more first compoundsout of the first multi-capillary column trap of the first trappingsystem in a second direction opposite the first direction; and transferone or more second compounds of the chemical sample and water vapor ofthe chemical sample from the first multi-capillary column trap to thesecond trapping system; the second trapping system including a packedtrap, the second trapping system configured to: trap, focus, andseparate the one or more second compounds of the chemical sample thatwere not retained by the first trapping system; while trapping,focusing, and separating the one or more second compounds of thechemical sample, remove the water vapor of the chemical sample, whereinthe water vapor traverses the packed trap prior to removal; and transferthe one or more second compounds of the chemical sample to one of theone or more detectors for chemical analysis, wherein the one or moresecond compounds and the water vapor traverse the first multi-capillarycolumn trap of the first trapping system before entering the secondtrapping system.
 2. The system of claim 1, wherein: the water vapor ofthe chemical sample is removed from the system both by lack of retentionby the packed trap and by purging the packed trap with an inert gas, andthe packed trap is configured to retain the one or more second compoundsduring the purging.
 3. The system of claim 1, wherein the secondtrapping system includes a focusing column, the focusing columnconfigured to: reduce a volume of the chemical sample, and remove thewater vapor of the chemical sample.
 4. The system of claim 3, whereinthe second trapping system further comprises a separating column fluidlycoupled to the focusing column, wherein transferring the one or moresecond compounds from the focusing column to the separating columncauses separation of the one or more second compounds.
 5. The system ofclaim 4, wherein the focusing column and the separating column areporous layer open tubular (PLOT) columns.
 6. The system of claim 1,wherein the one or more detectors is one detector, the detectorconfigured to conduct chemical analysis of the one or more firstcompounds and the one or more second compounds.
 7. The system of claim6, wherein the detector produces one chromatogram indicative of both theone or more first compounds and the one or more second compounds.
 8. Thesystem of claim 1, wherein: the second multi-capillary column trap ofthe first trapping system includes a first capillary column having afirst strength and a second capillary column having a second strengthhigher than the first strength, the first capillary column and thesecond capillary column are fluidly coupled, the first capillary columnis fluidly coupled to the one or more detectors, the second capillarycolumn is fluidly coupled to the second trapping system, the secondtrapping system is configured to transfer the one or more secondcompounds to the second capillary column of the second multi-capillarycolumn trap of the first trapping system after the one or more secondcompounds are separated, the second multi-capillary column trap isconfigured to facilitate transfer of the one or more second compoundsfrom the second trapping system to the one or more detectors while theone or more second compounds remain separated.
 9. The system of claim 8,wherein the second multi-capillary column trap is further configured toretain the one or more first compounds while the one or more secondcompounds are transferred to the second capillary column.
 10. The systemof claim 1, wherein the one or more second compounds include one or moreof ethane, ethylene, acetylene, formaldehyde, or a greenhouse gas.
 11. Amethod of analyzing a chemical sample, comprising: at a first trappingsystem that includes a first multi-capillary column trap and a secondmulti-capillary column trap: trapping, focusing, and separating one ormore first compounds of the chemical sample, including facilitating afirst flow of the one or more first compounds into the firstmulti-capillary column trap of the first trapping system in a firstdirection; transferring the one or more first compounds of the chemicalsample to one of one or more detectors for chemical analysis withoutallowing the one or more first compounds to traverse a second trappingsystem different from the first trapping system including facilitating asecond flow of the one or more first compounds out of the firstmulti-capillary column trap of the first trapping system in a seconddirection opposite the first direction; and transferring one or moresecond compounds of the chemical sample and water vapor of the chemicalsample from the first multi-capillary column trap to the second trappingsystem; at the second trapping system, the second trapping systemincluding a packed trap: trapping, focusing, and separating the one ormore second compounds of the chemical sample that were not retained bythe first trapping system; while trapping, focusing, and separating theone or more second compounds of the chemical sample, removing the watervapor of the chemical sample, wherein the water vapor traverses thepacked trap prior to removal; and transferring the one or more secondcompounds of the chemical sample to one of the one or more detectors forchemical analysis, wherein the one or more second compounds and thewater vapor traverse the first multi-capillary column trap of the firsttrapping system before entering the second trapping system.
 12. Themethod of claim 11, wherein the water vapor of the chemical sample isremoved from the second trapping system both by lack of retention by thepacked trap and by purging the packed trap with an inert gas, and thepacked trap is configured to retain the one or more second compoundsduring the purging.
 13. The method of claim 11, wherein the secondtrapping system includes a focusing column, and the method furthercomprises: reducing, at the focusing column, a volume of the chemicalsample, and removing the water vapor of the chemical sample.
 14. Themethod of claim 13, wherein the second trapping system further comprisesa separating column fluidly coupled to the focusing column, whereintransferring the one or more second compounds from the focusing columnto the separating column causes separation of the one or more secondcompounds.
 15. The method of claim 14, wherein the focusing column andthe separating column are porous layer open tubular (PLOT) columns. 16.The method of claim 11, wherein the one or more detectors is onedetector, and the method further comprises: performing chemical analysisof the one or more first compounds and the one or more second compoundswith the detector.
 17. The method of claim 16, further comprising:producing, with the detector, one chromatogram indicative of both theone or more first compounds and the one or more second compounds. 18.The method of claim 11, wherein: the second multi-capillary column trapof the first trapping system includes a first capillary column having afirst strength and a second capillary column having a second strengthhigher than the first strength, the first capillary column and thesecond capillary column are fluidly coupled, the first capillary columnis fluidly coupled to the one or more detectors, the second capillarycolumn is fluidly coupled to the second trapping system, and the methodfurther comprises: transferring, with the second trapping system, theone or more second compounds to the second capillary column of thesecond multi-capillary column trap after the one or more secondcompounds are separated; and facilitating, with the secondmulti-capillary column trap of the first trapping system, transfer ofthe one or more second compounds from the second trapping system to theone or more detectors while the one or more second compounds remainseparated.
 19. The method of claim 18, further comprising: retaining,with the second multi-capillary column trap, the one or more firstcompounds while the one or more second compounds are transferred to thesecond capillary column.
 20. The method of claim 11, wherein the one ormore second compounds include one or more of ethane, ethylene,acetylene, formaldehyde, or a greenhouse gas.